Michael W. Smith - Publications

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39 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2015 Iyengar SK, Sedor JR, Freedman BI, Kao WH, Kretzler M, Keller BJ, Abboud HE, Adler SG, Best LG, Bowden DW, Burlock A, Chen YD, Cole SA, Comeau ME, Curtis JM, ... ... Smith MW, et al. Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND). Plos Genetics. 11: e1005352. PMID 26305897 DOI: 10.1371/journal.pgen.1005352  0.92
2015 Turner TN, Sharma K, Oh EC, Liu YP, Collins RL, Sosa MX, Auer DR, Brand H, Sanders SJ, Moreno-De-Luca D, Pihur V, Plona T, Pike K, Soppet DR, Smith MW, et al. Loss of δ-catenin function in severe autism. Nature. 520: 51-6. PMID 25807484 DOI: 10.1038/nature14186  0.92
2013 Thameem F, Igo RP, Freedman BI, Langefeld C, Hanson RL, Schelling JR, Elston RC, Duggirala R, Nicholas SB, Goddard KA, Divers J, Guo X, Ipp E, Kimmel PL, Meoni LA, ... ... Smith MW, et al. A genome-wide search for linkage of estimated glomerular filtration rate (eGFR) in the Family Investigation of Nephropathy and Diabetes (FIND). Plos One. 8: e81888. PMID 24358131 DOI: 10.1371/journal.pone.0081888  0.92
2013 Alberg AJ, Jorgensen TJ, Ruczinski I, Wheless L, Shugart YY, Berthier-Schaad Y, Kessing B, Hoffman-Bolton J, Helzlsouer KJ, Kao WH, Francis L, Alani RM, Smith MW, Strickland PT. DNA repair gene variants in relation to overall cancer risk: a population-based study. Carcinogenesis. 34: 86-92. PMID 23027618 DOI: 10.1093/carcin/bgs304  0.92
2012 Jorgensen TJ, Ruczinski I, Yao Shugart Y, Wheless L, Berthier Schaad Y, Kessing B, Hoffman-Bolton J, Helzlsouer KJ, Kao WH, Francis L, Alani RM, Strickland PT, Smith MW, Alberg AJ. A population-based study of hedgehog pathway gene variants in relation to the dual risk of basal cell carcinoma plus another cancer. Cancer Epidemiology. 36: e288-93. PMID 22677152 DOI: 10.1016/j.canep.2012.05.001  0.92
2012 Ruczinski I, Jorgensen TJ, Shugart YY, Schaad YB, Kessing B, Hoffman-Bolton J, Helzlsouer KJ, Kao WH, Wheless L, Francis L, Alani RM, Strickland PT, Smith MW, Alberg AJ. A population-based study of DNA repair gene variants in relation to non-melanoma skin cancer as a marker of a cancer-prone phenotype. Carcinogenesis. 33: 1692-8. PMID 22581838 DOI: 10.1093/carcin/bgs170  0.92
2012 Wheless L, Kistner-Griffin E, Jorgensen TJ, Ruczinski I, Berthier-Schaad Y, Kessing B, Hoffman-Bolton J, Francis L, Shugart YY, Strickland PT, Kao WH, Alani RM, Smith MW, Alberg AJ. A community-based study of nucleotide excision repair polymorphisms in relation to the risk of non-melanoma skin cancer. The Journal of Investigative Dermatology. 132: 1354-62. PMID 22336945 DOI: 10.1038/jid.2012.4  0.92
2011 Igo RP, Iyengar SK, Nicholas SB, Goddard KA, Langefeld CD, Hanson RL, Duggirala R, Divers J, Abboud H, Adler SG, Arar NH, Horvath A, Elston RC, Bowden DW, Guo X, ... ... Smith MW, et al. Genomewide linkage scan for diabetic renal failure and albuminuria: the FIND study. American Journal of Nephrology. 33: 381-9. PMID 21454968 DOI: 10.1159/000326763  0.92
2010 Sezgin E, Jabs DA, Hendrickson SL, Van Natta M, Zdanov A, Lewis RA, Smith MW, Troyer JL, O'Brien SJ. Effect of host genetics on the development of cytomegalovirus retinitis in patients with AIDS. The Journal of Infectious Diseases. 202: 606-13. PMID 20617924 DOI: 10.1086/654814  0.92
2010 Winkler CA, Nelson GW, Smith MW. Admixture mapping comes of age. Annual Review of Genomics and Human Genetics. 11: 65-89. PMID 20594047 DOI: 10.1146/annurev-genom-082509-141523  0.92
2010 Sezgin E, Drosdak A, McIntosh C, Kessing B, Lautenberger JA, Goedert JJ, Phair JP, Troyer JL, Smith MW, O'Brien SJ. Examination of disease-based selection, demographic history and population structure in European Y-chromosome haplogroup I. Journal of Human Genetics. 55: 613-20. PMID 20574427 DOI: 10.1038/jhg.2010.77  0.92
2009 Chu AY, Parekh RS, Astor BC, Coresh J, Berthier-Schaad Y, Smith MW, Shuldiner AR, Kao WH. Association of APOE polymorphism with chronic kidney disease in a nationally representative sample: a Third National Health and Nutrition Examination Survey (NHANES III) Genetic Study. Bmc Medical Genetics. 10: 108. PMID 19852818 DOI: 10.1186/1471-2350-10-108  0.92
2009 Jorgensen TJ, Ruczinski I, Kessing B, Smith MW, Shugart YY, Alberg AJ. Hypothesis-driven candidate gene association studies: practical design and analytical considerations. American Journal of Epidemiology. 170: 986-93. PMID 19762372 DOI: 10.1093/aje/kwp242  0.92
2009 Tsilidis KK, Helzlsouer KJ, Smith MW, Grinberg V, Hoffman-Bolton J, Clipp SL, Visvanathan K, Platz EA. Association of common polymorphisms in IL10, and in other genes related to inflammatory response and obesity with colorectal cancer Cancer Causes and Control. 20: 1739-1751. PMID 19760027 DOI: 10.1007/s10552-009-9427-7  0.92
2009 Tishkoff SA, Reed FA, Friedlaender FR, Ehret C, Ranciaro A, Froment A, Hirbo JB, Awomoyi AA, Bodo JM, Doumbo O, Ibrahim M, Juma AT, Kotze MJ, Lema G, Moore JH, ... ... Smith MW, et al. The genetic structure and history of Africans and African Americans. Science (New York, N.Y.). 324: 1035-44. PMID 19407144 DOI: 10.1126/science.1172257  0.92
2009 Sperati CJ, Parekh RS, Berthier-Schaad Y, Jaar BG, Plantinga L, Fink N, Powe NR, Smith MW, Coresh J, Kao WH. Association of single-nucleotide polymorphisms in JAK3, STAT4, and STAT6 with new cardiovascular events in incident dialysis patients. American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation. 53: 845-55. PMID 19282076 DOI: 10.1053/j.ajkd.2008.12.025  0.92
2009 Wang MH, Helzlsouer KJ, Smith MW, Hoffman-Bolton JA, Clipp SL, Grinberg V, De Marzo AM, Isaacs WB, Drake CG, Shugart YY, Platz EA. Association of IL10 and other immune response- and obesity-related genes with prostate cancer in CLUE II Prostate. 69: 874-885. PMID 19267370 DOI: 10.1002/pros.20933  0.92
2009 Volfovsky N, Oleksyk TK, Cruz KC, Truelove AL, Stephens RM, Smith MW. Genome and gene alterations by insertions and deletions in the evolution of human and chimpanzee chromosome 22. Bmc Genomics. 10: 51. PMID 19171065 DOI: 10.1186/1471-2164-10-51  0.92
2009 Sezgin E, Lind JM, Shrestha S, Hendrickson S, Goedert JJ, Donfield S, Kirk GD, Phair JP, Troyer JL, O'Brien SJ, Smith MW. Association of Y chromosome haplogroup I with HIV progression, and HAART outcome. Human Genetics. 125: 281-94. PMID 19169712 DOI: 10.1007/s00439-008-0620-7  0.92
2008 Kopp JB, Smith MW, Nelson GW, Johnson RC, Freedman BI, Bowden DW, Oleksyk T, McKenzie LM, Kajiyama H, Ahuja TS, Berns JS, Briggs W, Cho ME, Dart RA, Kimmel PL, et al. MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis. Nature Genetics. 40: 1175-84. PMID 18794856 DOI: 10.1038/ng.226  0.92
2008 Kao WH, Klag MJ, Meoni LA, Reich D, Berthier-Schaad Y, Li M, Coresh J, Patterson N, Tandon A, Powe NR, Fink NE, Sadler JH, Weir MR, Abboud HE, Adler SG, ... ... Smith MW, et al. MYH9 is associated with nondiabetic end-stage renal disease in African Americans. Nature Genetics. 40: 1185-92. PMID 18794854 DOI: 10.1038/ng.232  0.92
2008 Oleksyk TK, Zhao K, De La Vega FM, Gilbert DA, O'Brien SJ, Smith MW. Identifying selected regions from heterozygosity and divergence using a light-coverage genomic dataset from two human populations Plos One. 3. PMID 18320033 DOI: 10.1371/journal.pone.0001712  0.92
2008 Schelling JR, Abboud HE, Nicholas SB, Pahl MV, Sedor JR, Adler SG, Arar NH, Bowden DW, Elston RC, Freedman BI, Goddard KA, Guo X, Hanson RL, Ipp E, Iyengar SK, ... ... Smith MW, et al. Genome-wide scan for estimated glomerular filtration rate in multi-ethnic diabetic populations: the Family Investigation of Nephropathy and Diabetes (FIND). Diabetes. 57: 235-43. PMID 18003762 DOI: 10.2337/db07-0313  0.92
2007 Iyengar SK, Abboud HE, Goddard KA, Saad MF, Adler SG, Arar NH, Bowden DW, Duggirala R, Elston RC, Hanson RL, Ipp E, Kao WH, Kimmel PL, Klag MJ, Knowler WC, ... ... Smith MW, et al. Genome-wide scans for diabetic nephropathy and albuminuria in multiethnic populations: the family investigation of nephropathy and diabetes (FIND). Diabetes. 56: 1577-85. PMID 17363742 DOI: 10.2337/db06-1154  0.92
2007 Zhang L, Kao WH, Berthier-Schaad Y, Plantinga L, Fink N, Smith MW, Coresh J. C-Reactive protein haplotype predicts serum C-reactive protein levels but not cardiovascular disease risk in a dialysis cohort. American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation. 49: 118-26. PMID 17185152 DOI: 10.1053/j.ajkd.2006.10.008  0.92
2007 Lind JM, Hutcheson-Dilks HB, Williams SM, Moore JH, Essex M, Ruiz-Pesini E, Wallace DC, Tishkoff SA, O'Brien SJ, Smith MW. Elevated male European and female African contributions to the genomes of African American individuals. Human Genetics. 120: 713-22. PMID 17006671 DOI: 10.1007/s00439-006-0261-7  0.92
2006 Liu Y, Berthier-Schaad Y, Plantinga L, Fink NE, Tracy RP, Kao WH, Klag MJ, Smith MW, Coresh J. Functional variants in the lymphotoxin-alpha gene predict cardiovascular disease in dialysis patients. Journal of the American Society of Nephrology : Jasn. 17: 3158-66. PMID 16988060 DOI: 10.1681/ASN.2006030299  0.92
2006 Shrestha S, Smith MW, Broman KW, Farzadegan H, Vlahov D, Strathdee SA. Multiperson use of syringes among injection drug users in a needle exchange program: a gene-based molecular epidemiologic analysis. Journal of Acquired Immune Deficiency Syndromes (1999). 43: 335-43. PMID 16980914 DOI: 10.1097/01.qai.0000230528.25083.0b  0.92
2006 Zhang L, Kao WH, Berthier-Schaad Y, Liu Y, Plantinga L, Jaar BG, Fink N, Powe N, Klag MJ, Smith MW, Coresh J. Haplotype of signal transducer and activator of transcription 3 gene predicts cardiovascular disease in dialysis patients. Journal of the American Society of Nephrology : Jasn. 17: 2285-92. PMID 16807407 DOI: 10.1681/ASN.2005090985  0.92
2006 Liu Y, Berthier-Schaad Y, Fallin MD, Fink NE, Tracy RP, Klag MJ, Smith MW, Coresh J. IL-6 haplotypes, inflammation, and risk for cardiovascular disease in a multiethnic dialysis cohort. Journal of the American Society of Nephrology : Jasn. 17: 863-70. PMID 16467451 DOI: 10.1681/ASN.2005050465  0.92
2006 Shrestha S, Strathdee SA, Broman KW, Smith MW. Unknown biological mixtures evaluation using STR analytical quantification. Electrophoresis. 27: 409-15. PMID 16437418 DOI: 10.1002/elps.200500502  0.92
2006 Shrestha S, Strathdee SA, Galai N, Oleksyk T, Fallin MD, Mehta S, Schaid D, Vlahov D, O'Brien SJ, Smith MW. Behavioral risk exposure and host genetics of susceptibility to HIV-1 infection. The Journal of Infectious Diseases. 193: 16-26. PMID 16323127 DOI: 10.1086/498532  0.92
2005 Smith MW, O'Brien SJ. Mapping by admixture linkage disequilibrium: Advances, limitations and guidelines Nature Reviews Genetics. 6: 623-632. PMID 16012528 DOI: 10.1038/nrg1657  0.92
2005 Liu Y, Berthier-Schaad Y, Fink NE, Fallin MD, Tracy RP, Klag MJ, Smith MW, Coresh J. Beta-fibrinogen haplotypes and the risk for cardiovascular disease in a dialysis cohort. American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation. 46: 78-85. PMID 15983960 DOI: 10.1053/j.ajkd.2005.03.008  0.92
2005 Shrestha S, Smith MW, Beaty TH, Strathdee SA. Theory and methodology for utilizing genes as biomarkers to determine potential biological mixtures. Annals of Epidemiology. 15: 29-38. PMID 15571991 DOI: 10.1016/j.annepidem.2004.05.006  0.92
2004 Winkler CA, Hendel H, Carrington M, Smith MW, Nelson GW, O'brien SJ, Phair J, Vlahov D, Jacobson LP, Rappaport J, Vasilescu A, Bertin-Maghit S, An P, Lu W, Andrieu JM, et al. Dominant effects of CCR2-CCR5 haplotypes in HIV-1 disease progression. Journal of Acquired Immune Deficiency Syndromes (1999). 37: 1534-8. PMID 15602133 DOI: 10.1097/01.qai.0000127353.01578.63  0.92
2004 Smith MW, Patterson N, Lautenberger JA, Truelove AL, McDonald GJ, Waliszewska A, Kessing BD, Malasky MJ, Scafe C, Le E, De Jager PL, Mignault AA, Yi Z, De The G, Essex M, et al. A high-density admixture map for disease gene discovery in african americans. American Journal of Human Genetics. 74: 1001-13. PMID 15088270 DOI: 10.1086/420856  0.92
2004 Patterson N, Hattangadi N, Lane B, Lohmueller KE, Hafler DA, Oksenberg JR, Hauser SL, Smith MW, O'Brien SJ, Altshuler D, Daly MJ, Reich D. Methods for high-density admixture mapping of disease genes. American Journal of Human Genetics. 74: 979-1000. PMID 15088269 DOI: 10.1086/420871  0.92
2003 Breen EC, Boscardin WJ, Detels R, Jacobson LP, Smith MW, O'Brien SJ, Chmiel JS, Rinaldo CR, Lai S, Martínez-Maza O. Non-Hodgkin's B cell lymphoma in persons with acquired immunodeficiency syndrome is associated with increased serum levels of IL10, or the IL10 promoter -592 C/C genotype. Clinical Immunology (Orlando, Fla.). 109: 119-29. PMID 14597210 DOI: 10.1016/S1521-6616(03)00214-6  0.92
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